In this study we determined serum IL-8 levels in 18 untransfused patie
nts with beta-thalassemia intermedia and in 14 subjects affected by Hb
H disease. As reported in polytransfused homozygous beta-thalassemia,
untransfused beta-thalassemia and HbH disease show significantly (p<0.
005) higher serum IL-8 levels than normal controls. Our data suggest t
hat there could be an intrinsic cause for the IL-8 increase in thalass
emia intermedia. We think that the hyperactivity of thalassemic macrop
hages related to chronic hemolysis is the main cause for the increment
in cytokines, such as IL-8, found in thalassemic syndromes.